Canonical Allele Identifier: CA2628140829
Gene: STRC HGNC NCBI
CKMT1B HGNC NCBI

Linked Data

gnomAD v4: 15-43599594-A-T
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.43599594A>T , CM000677.2:g.43599594A>T GRCh38
NC_000015.9:g.43891792A>T , CM000677.1:g.43891792A>T GRCh37
NC_000015.8:g.41679084A>T NCBI36
NG_011636.1:g.24207T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000450892.7:c.*78T>A (STRC) MANE Select ENSP00000401513.2:n.*78T>A
ENST00000411560.1:n.142+61A>T (CKMT1B)
ENST00000450892.6:c.*78T>A (STRC) ENSP00000401513.2:n.*78T>A
ENST00000471703.5:n.3360T>A (STRC)
ENST00000541030.5:c.*78T>A (STRC) ENSP00000440413.1:n.*78T>A
NM_153700.2:c.*78T>A (STRC) MANE Select NP_714544.1:n.*78T>A
XM_011521277.1:c.*78T>A (STRC) XP_011519579.1:n.*78T>A
XM_011521278.1:c.*78T>A (STRC) XP_011519580.1:n.*78T>A
XM_011521279.1:c.*78T>A (STRC) XP_011519581.1:n.*78T>A
Search 100 bp 5'
Search 100 bp 3'